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Second tyrosine kinase inhibitor discontinuation attempt in patients with chronic myeloid leukemia.
Legros, Laurence; Nicolini, Franck E; Etienne, Gabriel; Rousselot, Philippe; Rea, Delphine; Giraudier, Stéphane; Guerci-Bresler, Agnès; Huguet, Françoise; Gardembas, Martine; Escoffre, Martine; Ianotto, Jean-Christophe; Noël, Marie-Pierre; Varet, Bruno R; Pagliardini, Thomas; Touitou, Irit; Morisset, Stéphane; Mahon, Francois-Xavier.
Afiliação
  • Legros L; Hematology Department, Nice University Hospital, Nice, France.
  • Nicolini FE; Valrose Institute of Biology, National Center for Scientific Research (CNRS) Unit 7277, National Institute of Health and Medical Research (INSERM) Unit 1091, Nice, France.
  • Etienne G; Hematology Department, Lyon University Hospital, Pierre Benite, France.
  • Rousselot P; INSERM Unit 1052, Leon Berard Center, Lyon, France.
  • Rea D; Haematology Department, Bergonie Institute, Bordeaux, France.
  • Giraudier S; Haematology and Oncology Department, Hopital A Mignot, INSERM Unit 1173, Versailles, University of Versailles St.-Quentin-Yvelines, France.
  • Guerci-Bresler A; Adult Hematology Department, INSERM Unit 1160, St. Louis Hospital, Paris, France.
  • Huguet F; Hematology Laboratory, Henri-Mondor Hospital, Creteil, France.
  • Gardembas M; Hematology Department, Brabois University Hospital, Vandoeuvre-les-Nancy, France.
  • Escoffre M; Hematology Department, Toulouse-Oncopole University Cancer Institute, Toulouse, France.
  • Ianotto JC; Blood Disorder Department, Angers University Hospital, Angers, France.
  • Noël MP; Adult Hematology Department, Rennes University Hospital, Rennes, France.
  • Varet BR; Hematology Department, Brest University Hospital, Brest, France.
  • Pagliardini T; Blood Disorders Department, Lille University Hospital, Lille, France.
  • Touitou I; Blood Disorders Department, Necker Hospital, Paris-Descartes University, Paris, France.
  • Morisset S; Hematology Department, Nice University Hospital, Nice, France.
  • Mahon FX; Hematology Department, Nice University Hospital, Nice, France.
Cancer ; 123(22): 4403-4410, 2017 Nov 15.
Article em En | MEDLINE | ID: mdl-28743166
ABSTRACT

BACKGROUND:

Several studies have demonstrated that approximately one-half of patients with chronic myeloid leukemia (CML) who receive treatment with tyrosine kinase inhibitors (TKIs) and achieve and maintain a deep molecular response (DMR) are able to successfully discontinue therapy. In patients who have a molecular relapse, a DMR is rapidly regained upon treatment re-initiation.

METHODS:

The authors report the results from RE-STIM, a French observational, multicenter study that evaluated treatment-free remission (TFR) in 70 patients who re-attempted TKI discontinuation after a first unsuccessful attempt. After the second TKI discontinuation attempt, the trigger for treatment re-introduction was the loss of a major molecular response in all patients.

RESULTS:

The median follow-up was 38.3 months (range, 4.7-117 months), and 45 patients (64.3%) lost a major molecular response after a median time off therapy of 5.3 months (range, 2-42 months). TFR rates at 12, 24, and 36 months were 48% (95% confidence interval [CI], 37.6%-61.5%), 42% (95% CI, 31.5%-55.4%), and 35% (95% CI, 24.4%-49.4%), respectively. No progression toward advanced-phase CML occurred, and no efficacy issue was observed upon TKI re-introduction. In univariate analysis, the speed of molecular relapse after the first TKI discontinuation attempt was the only factor significantly associated with outcome. The TFR rate at 24 months was 72% (95% CI, 48.8%-100%) in patients who remained in DMR within the first 3 months after the first TKI discontinuation and 36% (95% CI, 25.8%-51.3%) for others.

CONCLUSIONS:

This study is the first to demonstrate that a second TKI discontinuation attempt is safe and that a first failed attempt at discontinuing TKI does not preclude a second successful attempt. Cancer 2017;1234403-10. © 2017 American Cancer Society.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Inibidores de Proteínas Quinases Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Leucemia Mielogênica Crônica BCR-ABL Positiva / Inibidores de Proteínas Quinases Tipo de estudo: Clinical_trials / Observational_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Cancer Ano de publicação: 2017 Tipo de documento: Article